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Author/Creator Schwartz, Ida V. D.

1. Adenosine kinase deficiency presenting with tortuous cervical arteries: A risk factor for recurrent stroke. Issue 1 (30th September 2021)

Authors:
Paz, José A.; Embiruçu, Emilia K.; Bueno, Clarissa; Ferreira, Rafaela C. C. L.; Oliveira, Fernanda S.; Pereira, Ane S. S.; Schwartz, Ida V. D.; Paiva, Anderson R. B.; Lucato, Leandro T.; Kok, Fernando
Journal:
JIMD reports
Issue:
Volume 62:Issue 1(2021)
Page Start:
49
Record Type:
Journal Article
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2. ALG6‐CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. Issue 5 (10th June 2016)

Authors:
Morava, Eva; Tiemes, Vera; Thiel, Christian; Seta, Nathalie; de Lonlay, Pascale; de Klerk, Hans; Mulder, Margot; Rubio‐Gozalbo, Estela; Visser, Gepke; van Hasselt, Peter; Horovitz, Dafne D. G.; de Souza, Carolina Fischinger Moura; Schwartz, Ida V. D.; Green, Andrew; Al‐Owain, Mohammed; Uziel, Gra...
Journal:
Journal of inherited metabolic disease
Issue:
Volume 39:Issue 5(2016)
Page Start:
713
Record Type:
Journal Article
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4. Diagnosis and Management of Classical Homocystinuria in Brazil: A Summary of 72 Late-Diagnosed Patients. (7th August 2018)

Authors:
Poloni, Soraia; Hoss, Giovana W.; Sperb-Ludwig, Fernanda; Borsatto, Taciane; Doriqui, Maria Juliana R.; Leão, Emília K.E.A; Boa-Sorte, Ney; Lourenço, Charles M.; Kim, Chong A.; de Souza, Carolina F. M.; Rocha, Helio; Ribeiro, Marcia; Steiner, Carlos E.; Moreno, Carolina A.; Bernardi, Pricila; Val...
Journal:
Journal of inborn errors of metabolism and screening
Issue:
Volume 6(2018)
Page Start:
Record Type:
Journal Article
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6. Erratum to: ALG6‐CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies. Issue 5 (8th August 2016)

Authors:
Morava, Eva; Tiemes, Vera; Thiel, Christian; Seta, Nathalie; de Lonlay, Pascale; de Klerk, Hans; Mulder, Margot; Rubio‐Gozalbo, Estela; Visser, Gepke; van Hasselt, Peter; Horovitz, Dafne D. G.; de Souza, Carolina Fischinger Moura; Schwartz, Ida V. D.; Green, Andrew; Al‐Owain, Mohammed; Uziel, Gra...
Journal:
Journal of inherited metabolic disease
Issue:
Volume 39:Issue 5(2016)
Page Start:
759
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

7. Erratum to: In vitro digestion of starches in a dynamic gastrointestinal model: an innovative study to optimize dietary management of patients with hepatic glycogen storage diseases. Issue 5 (20th May 2015)

Authors:
Nalin, Tatiéle; Venema, Koen; Weinstein, David A.; de Souza, Carolina F. M; Perry, Ingrid D. S.; van Wandelen, Mario T. R.; van Rijn, Margreet; Smit, G. Peter A.; Schwartz, Ida V. D.; Derks, Terry G. J.
Journal:
Journal of inherited metabolic disease
Issue:
Volume 38:Issue 5(2015)
Page Start:
987
Record Type:
Journal Article
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8. In vitro digestion of starches in a dynamic gastrointestinal model: an innovative study to optimize dietary management of patients with hepatic glycogen storage diseases. Issue 3 (16th September 2014)

Authors:
Nalin, Tatiéle; Venema, Koen; Weinstein, David A.; de Souza, Carolina F. M; Perry, Ingrid D. S.; van Wandelen, Mario T. R.; van Rijn, Margreet; Smit, G. Peter A.; Schwartz, Ida V. D.; Derks, Terry G. J.
Journal:
Journal of inherited metabolic disease
Issue:
Volume 38:Issue 3(2015)
Page Start:
529
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗